Allele Registry

Canonical Allele Identifier: PA119027

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008190

RCV002512895

ClinVar Variation:

7749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017535.1:p.Arg80Gln	CA119026 NM_001017535.2:c.239G>A